Canonical Allele Identifier: PA2830264781
Gene: FLCN HGNC NCBI

Linked Data

ClinVar Variation Id: 2905593
ClinVar RCV Id: RCV003607055

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_659434.2:p.Glu530Val
CA398530424
NM_144997.7:c.1589A>T